VLADMIVA Pulpevit - Indonesia BPOM Medical Device Registration
VLADMIVA Pulpevit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602420128. The device is manufactured by JSC EXPERIMENTAL PLANT VLADMIVA from Russia, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TRI ANUGERAH JAYA.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Manufacturer
JSC EXPERIMENTAL PLANT VLADMIVACountry of Origin
Russia
Authorized Representative
PT. TRI ANUGERAH JAYAAR Address
Jl. Raya Pos Pengumben 34 G, RT/RW 002/005
Registration Date
Mar 05, 2024
Expiry Date
Jul 14, 2028
Product Type
Prosthetic Dental Equipment
Root canal filling resin
Non Electromedic Non Sterile
VLADMIVA Trioxident
VLADMIVA Cresodent
VLADMIVA DEVIT-S
VLADMIVA ALVANES
VLADMIVA Eodent
VLADMIVA Pulpevit
DEVIT-ARS
VLADMIVA Tiedent
VLADMIVA Cresodent
VLADMIVA Pulpodent
MLG Camera Intra Oral
MLG MEDICAL INSTRUMENT(SHENZHEN)CO., LTD.
RTA i LED II
GUILIN WOODPECKER MEDICAL INSTRUMENT CO., LTD.
PERFECT Endo Motor BR-Rap
SHANWEI PERFECT MEDICAL INSTRUMENTS CO., LTD
PEARL ENDOPIA Gutta Percha Point
PEARL DENT CO., LTD.
FGM pleaded
DENTSCARE LTDA
RTD Matchpost
R.T.D. (DENTAL TECHNICAL RESEARCH)
VLADMIVA Trioxident
JSC EXPERIMENTAL PLANT VLADMIVA
i-Dental i-Flow N
JSC MEDICINOS LINIJA
VLADMIVA Pulpodent
JSC EXPERIMENTAL PLANT VLADMIVA
i-Seal LC Light Curing Pit and Fissure Sealant
JSC MEDICINOS LINIJA

